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Filtered Search Results
Chem-Impex International, Inc. Pentamethylcyclopentadienylrhodium(III) chloride dimer | MFCD00061552 | 100MG
Pentamethylcyclopentadienylrhodium(III) chloride dimer, MFCD00061552, 100MG
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![eMolecules AstaTech / PENTAMETHYLCYCLOPENTADIENYLRHODIUM(III) CHLORIDE DIMER / 0.25g / 449765095 / F20614 / 95.000 / 12354-85-7 / [null] / 618.070 / C20H30Cl4Rh2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502465778.JPG-250.jpg)
eMolecules AstaTech / PENTAMETHYLCYCLOPENTADIENYLRHODIUM(III) CHLORIDE DIMER / 0.25g / 449765095 / F20614 / 95.000 / 12354-85-7 / [null] / 618.070 / C20H30Cl4Rh2
AstaTech / PENTAMETHYLCYCLOPENTADIENYLRHODIUM(III) CHLORIDE DIMER / 0.25g / 449765095 / F20614 / 95.000 / 12354-85-7 / [null] / 618.070 / C20H30Cl4Rh2
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eMolecules 1-Phenyl-1-hexyne | 1129-65-3 | 5G | Purity: 98%
Combi-Blocks | 1-Phenyl-1-hexyne | 5G | 1129-65-3 | MFCD00039969
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Apexbio Technology LLC I-BET-762 1260907-17-2 5mg
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I-BET-762 (CAS 1260907-17-2) is a small-molecule inhibitor targeting the BET (bromodomain and extra-terminal) family of proteins It acts by competitively binding to the acetyl-lysine recognition pocket of BET bromodomains thereby displacing acetylated histones with an IC50 ranging from 32 5 to 42 5 nM and a dissociation constant (Kd) between 50 5 and 61 3 nM I-BET-762 displays high selectivity exhibiting no interaction with non-BET bromodomain-containing proteins In cellular studies it downregulates LPS-induced gene expression resulting in reduced production of pro-inflammatory cytokines and chemokines In vivo models demonstrate its potential to attenuate features of established inflammatory disease supporting its utility in epigenetic and inflammation-related research
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![eMolecules ChemScene / 1357-tetrakis(4-iodophenyl)adamantane / 250mg / 626491939 / CS-0146174 / 0.000 / 144970-30-9 / [null] / 944.216 / C34H28I4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502483756.JPG-250.jpg)
eMolecules ChemScene / 1357-tetrakis(4-iodophenyl)adamantane / 250mg / 626491939 / CS-0146174 / 0.000 / 144970-30-9 / [null] / 944.216 / C34H28I4
ChemScene / 1357-tetrakis(4-iodophenyl)adamantane / 250mg / 626491939 / CS-0146174 / 0.000 / 144970-30-9 / [null] / 944.216 / C34H28I4
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eMolecules 1-Phenyl-1-butyne | 622-76-4 | MFCD00039945 | 5g
Combi-Blocks, Inc. | 1-Phenyl-1-butyne | 5g | 569297606 | QF-0593 | 95.000 | 622-76-4 | MFCD00039945 | 130.190 | C10H10
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Medchemexpress LLC DI-591 | 2245887-38-9 | 98.06% | 585.80 | 5 MG
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DI-591 is a potent, high-affinity, and cell-permeable inhibitor of the DCN1-UBC12 interaction. It selectively inhibits the neddylation of cullin 3, with minimal or no effect on other cullin family members.
- Binds to DCN1 and DCN2 with Ki values of 12 nM and 10.4 nM, respectively
- Shows no significant binding to DCN3, DCN4, and DCN5 proteins
- Serves as an excellent probe compound for investigating the role of cullin 3 CRL
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Medchemexpress LLC DI-591 | 2245887-38-9 | 98.4% | 585.80 | C31H47N5O4S | 50MG
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DI-591 is a potent, cell-permeable small-molecule inhibitor of the DCN1-UBC12 interaction that blocks cullin 3 neddylation. It is intended for biochemical and cellular research where inhibition of neddylation and modulation of ubiquitin-pathway signaling are required.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000429578 CY7-YNE 25MG
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Sigma Aldrich Fine Chemicals Biosciences 1 Heptyne 98
The hydrogenation of 1-heptyne with palladium platinum and ruthenium supported on activated carbon as catalysts was studied.
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eMolecules 4,6-O-Ethylidene-a-D-glucose | 13224-99-2 | MFCD00006820 | 25g
Chem-Impex | 4,6-O-Ethylidene-a-D-glucose | 25g | 526509973 | 32262 | | 13224-99-2 | MFCD00006820 | 206.194 | C8H14O6
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Medchemexpress LLC ML162-yne | 2883115-46-4 | C25H22Cl2N2O3S | 10 MM 1 ML
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ML162-yne is a potent GPX4-inhibitor affinity probe. It is a click chemistry reagent containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Potent GPX4 inhibitor
- Affinity probe
- Click chemistry reagent
- Contains alkyne group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc)
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Medchemexpress LLC DI-591 | 2245887-38-9 | 98.4% | 585.80 | 10 MG
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DI-591 is a potent, high-affinity, and cell-permeable inhibitor of the DCN1-UBC12 interaction. It selectively inhibits neddylation of cullin 3 with minimal effect on other cullin family members, making it an excellent probe compound for investigating the role of cullin 3 CRL in biological processes and human diseases. It also leads to NRF2 protein accumulation and transcriptional activation.
- Binds to DCN1 and DCN2 with high affinity (Ki values of 12 nM and 10.4 nM respectively)
- Shows >1000-fold selectivity over recombinant human DCN3-5 proteins
- Disrupts the association of cellular DCN1 and UBC12 proteins
- Increases mRNA levels of NQO1 and HO1
- Used for research purposes only
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eMolecules 1-AMINO-3-CYCLOPENTENE HYD 10G
5000217099 1-AMINO-3-CYCLOPENTENE HYD 10G
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Sigma Aldrich Fine Chemicals Biosciences Cyclohexene inhibitor-free, ReagentPlus(R), 99% | 110-83-8 | MFCD00001539 | 1L
Cyclohexene inhibitor-free, ReagentPlus(R), 99% | Purity: 99% | Mol Wt: 82.14 | 110-83-8 | MFCD00001539 | 1L
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